EP4246608A1 - Flüssigzusammensetzung, behälter, elektrochemisches element, verfahren und vorrichtung - Google Patents

Flüssigzusammensetzung, behälter, elektrochemisches element, verfahren und vorrichtung Download PDF

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Publication number
EP4246608A1
EP4246608A1 EP23160337.4A EP23160337A EP4246608A1 EP 4246608 A1 EP4246608 A1 EP 4246608A1 EP 23160337 A EP23160337 A EP 23160337A EP 4246608 A1 EP4246608 A1 EP 4246608A1
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EP
European Patent Office
Prior art keywords
liquid composition
electrochemical device
polymer
manufacturing
mass
Prior art date
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EP23160337.4A
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English (en)
French (fr)
Inventor
Kayato OHYA
Toshiya Sagisaka
Soh Noguchi
Satoshi Nakajima
Hiromichi KURIYAMA
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Ricoh Co Ltd
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Ricoh Co Ltd
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Publication date
Priority claimed from JP2022206669A external-priority patent/JP2023135606A/ja
Application filed by Ricoh Co Ltd filed Critical Ricoh Co Ltd
Publication of EP4246608A1 publication Critical patent/EP4246608A1/de
Pending legal-status Critical Current

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    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M4/04—Processes of manufacture in general
    • H01M4/0402—Methods of deposition of the material
    • H01M4/0404—Methods of deposition of the material by coating on electrode collectors
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00—Secondary cells; Manufacture thereof
    • H01M10/05—Accumulators with non-aqueous electrolyte
    • H01M10/052—Li-accumulators
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00—Secondary cells; Manufacture thereof
    • H01M10/05—Accumulators with non-aqueous electrolyte
    • H01M10/056—Accumulators with non-aqueous electrolyte characterised by the materials used as electrolytes, e.g. mixed inorganic/organic electrolytes
    • H01M10/0561—Accumulators with non-aqueous electrolyte characterised by the materials used as electrolytes, e.g. mixed inorganic/organic electrolytes the electrolyte being constituted of inorganic materials only
    • H01M10/0562—Solid materials
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00—Secondary cells; Manufacture thereof
    • H01M10/05—Accumulators with non-aqueous electrolyte
    • H01M10/058—Construction or manufacture
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M4/13—Electrodes for accumulators with non-aqueous electrolyte, e.g. for lithium-accumulators; Processes of manufacture thereof
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M4/13—Electrodes for accumulators with non-aqueous electrolyte, e.g. for lithium-accumulators; Processes of manufacture thereof
    • H01M4/139—Processes of manufacture
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M4/62—Selection of inactive substances as ingredients for active masses, e.g. binders, fillers
    • H01M4/621—Binders
    • H01M4/622—Binders being polymers
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/10—Energy storage using batteries

Definitions

  • the present disclosure is related to a liquid composition, a liquid composition for inkjet discharging, a container, a device for manufacturing an electrochemical device's part, a device for manufacturing an electrochemical device, a method of manufacturing an electrochemical device's part, a method of manufacturing an electrochemical device, and an electrochemical device.
  • Electrochemical devices including secondary batteries such as lithium ion secondary batteries, are mounted on portable devices, hybrid vehicles, and electric vehicles.
  • the demand for such a device is increasing.
  • the need for a wearable device and a medical patch carrying a thin battery is increasing, diversifying demand for secondary batteries.
  • a liquid composition for an electrode mixture layer generally contains an active material, a dispersant, and a binder for enhancing a binding affinity with an obtained electrode mixture layer.
  • the binder is generally a polymer and the liquid composition for an electrode mixture is prepared to have a high solid content concentration to increase the productivity.
  • the liquid composition for an electrode mixture is thus a slurry with an extremely high viscosity, from 10 3 to 10 4 mPa ⁇ s. Therefore, electrodes constituting a lithium ion secondary battery are typically manufactured by applying a liquid composition for an electrode mixture layer to an electrode substrate using a die coater, a comma coater, or a reverse roll coater, thereby forming an electrode mixture layer on the substrate.
  • a method of manufacturing such a secondary battery by applying a liquid composition for an electrode mixture layer using inkjet printing which executes an intermittent application easily, is appealing to reduce the material cost and the environmental burden.
  • inkjet printing is generally suitable for applying a liquid composition with a low viscosity.
  • the upper limit of viscosity is 200 mPa ⁇ s, which is a viscosity level at a factor of from 1:10 to 1:100 of that of a typical slurry liquid composition for an electrode mixture layer.
  • liquid composition for an electrode mixture layer with a low viscosity As a liquid composition for an electrode mixture layer with a low viscosity, a liquid composition for an electrode mixture layer for inkjet printing with a viscosity of from 3.1 to 5.8 mPa ⁇ s has been proposed in Examples of Japanese Unexamined Patent Application Publication No.2009-152180 .
  • the liquid composition contains a binder with a viscosity of from 1 to 20 mPa ⁇ s in an aqueous solution at 1 percent by mass.
  • the proportion of the binder is from 0.01 to 0.5 percent by mass in the liquid composition.
  • a slurry composition for an electrode mixture layer with a solid content as high as 75 percent by mass or greater as a binder composition for a non-aqueous secondary battery containing a binder material and an organic solvent has been proposed in WO2019/044452 .
  • the slurry composition is prepared using a binder composition for a non-aqueous secondary battery electrode with a viscosity of 10,000 mPa ⁇ s or less at a shearing speed of 0.1 s -1 for a mixture obtained by mixing a polymer A at a concentration of 8 percent by mass and the organic solvent mentioned above.
  • the binder contains the polymer A, and the polymer A has an ethylenic unsaturated acid monomer unit of from 1.00 to 10.00 percent by mass.
  • a liquid composition which has a high solid content concentration while having a viscosity low enough for inkjet printing and can form an electrochemical device's part with a layer containing an ion conductive material with a high resistance to peeling.
  • a liquid composition which contains an ion conductive material, a dispersant, a polymer, and a solvent, wherein the polymer contains a (meth)acrylate-based polymer containing a (meth)acrylic acid alkyl ester monomer and the (meth)acrylate-based polymer has a glass transition temperature of 80 degrees C or lower, wherein a liquid mixture of the polymer and the solvent where the concentration of the polymer is 10 percent by mass has a viscosity of 50 mPa ⁇ s or less at 25 degrees C.
  • a liquid composition for inkjet discharging which contains the liquid composition mentioned above.
  • a container which contains the liquid composition mentioned above.
  • a device for manufacturing an electrochemical device's part which includes the container mentioned above and a discharging device including an inkjet head for discharging the liquid composition in the container.
  • a device for manufacturing an electrochemical device which includes a unit for manufacturing an electrochemical device's part with the device for manufacturing an electrochemical device's part.
  • a method of manufacturing an electrochemical device's part includes discharging the liquid composition mentioned above using an inkjet head provided.
  • a method of manufacturing an electrochemical device which includes manufacturing an electrochemical device's part by the method of manufacturing an electrochemical device's part mentioned above.
  • an electrochemical device which includes a current collector and a layer containing an ion conductive material, a dispersant, and a polymer, wherein the polymer contains a (meth)acrylate-based polymer comprising a (meth)acrylic acid alkyl ester monomer and the (meth)acrylate-based polymer has a glass transition temperature of 80 degrees C or lower, wherein a liquid mixture of the polymer and a solvent where a concentration of the polymer is 10 percent by mass has a viscosity of 50 mPa ⁇ s or less at 25 degrees C.
  • recording media, media, and print substrates in the present disclosure have the same meaning unless otherwise specified.
  • the liquid composition of the present disclosure is used for forming an electrochemical device's part and contains an ion conductive material, a dispersant, a polymer, and a solvent.
  • the composition may furthermore optionally contain other components.
  • a liquid composition for an electrode mixture layer for inkjet printing has been proposed in Japanese Unexamined Patent Application Publication No. 2009-152180 .
  • the productivity of this liquid composition is relatively low compared to that of a typical slurry liquid composition for electrode mixture, considering that the liquid composition has a low solid content concentration, only 20 to 40 percent by mass, while the slurry liquid composition has a solid content concentration of from 60 to 70 percent by mass.
  • the slurry composition for an electrode mixture proposed in WO2019/044452 is required to be diluted to a solid content concentration lower than that of the typical slurry liquid composition mentioned above in order to use the slurry composition for inkjet printing.
  • the layer containing an ion conductive material obtained such as an electrode mixture layer or solid electrolyte layer cannot have a sufficient binding property.
  • the layer containing an ion conductive material is thus not sufficiently resistant to peeling.
  • More improvements are desired to achieve a high solid content concentration and a low viscosity suitable for inkjet printing on a par with those of a typical liquid slurry composition for a secondary battery and obtain a layer containing an ion conductive material with sufficient resistance to peeling.
  • the liquid composition of the present disclosure is used to form an electrochemical device's part, such as an electrode or solid electrolyte layer of a secondary battery.
  • the liquid composition for forming an electrode of a secondary battery can be used to form an electrode of a non-aqueous secondary battery such as a lithium ion secondary battery.
  • the liquid composition for forming a solid electrolyte layer of a secondary battery can be used to form a solid electrolyte layer of a non-aqueous secondary battery such as a lithium ion secondary battery.
  • the polymer is a (meth)acrylate-based polymer with a glass transition temperature of 80 degrees C or lower containing a (meth)acrylic acid alkyl ester monomer.
  • a liquid mixture of the polymer and the solvent mentioned above in which the concentration of the polymer is 10 percent by mass has a viscosity of 50 mPa ⁇ s or less at 25 degrees C.
  • the polymer is mixed in the range of concentration by mass in which the polymer is dissolved in the solvent.
  • the polymer has compatibility with the solvent. Specifically, precipitates or supernatant are not visually confirmed in this range when a (meth)acrylate-based polymer is charged and dissolved in the solvent mentioned above at 25 degrees C, followed by standing for 10 minutes.
  • the conditions under which the polymer is dissolved is not particularly limited as long as the polymer is dissolved.
  • the polymer does not excessively increase the viscosity of the liquid composition mentioned above.
  • the polymer holds the components in an electrode mixture layer, not to be detached from the electrode mixture layer; in other words, acting as a binding material when an electrode is manufactured by forming the electrode mixture layer on a current collector using the liquid composition,
  • the polymer holds the components in a solid electrolyte layer, not to be detached from a laminate manufactured by forming the solid electrolyte layer on an electrode using the liquid composition.
  • the polymer contains a (meth)acrylic acid alkyl ester monomer with weak adsorption energy to an ion conductive material compared to a dispersant for an ion conductive material, which is described later.
  • the polymer is thus unlikely to inhibit the dispersant for an ion conductive material from adsorbing the ion conductive material. Therefore, the ion conductive material is unlikely to agglomerate in an organic solvent so that the liquid composition of the present disclosure has an extremely low viscosity while having a high solid content concentration.
  • whether a (meth)acrylic acid alkyl ester monomer is present can be measured by nuclear magnetic resonance (NMR) such as 1 H-NMR.
  • NMR nuclear magnetic resonance
  • the (meth)acrylic acid alkyl ester monomer has a linear alkyl group or a branched alkyl group.
  • Specific examples of the (meth) acrylic acid ester monomer include, but are not limited to, acrylic acid alkyl esters such as methyl acrylate, ethyl acrylate, n-propyl acrylate, isopropyl acrylate, n-butyl acrylate, t-butyl acrylate, pentyl acrylate, hexyl acrylate, heptyl acrylate, octyl acrylate, 2-ethylhexyl acrylate, nonyl acrylate, decyl acrylate, lauryl acrylate, n-tetradecyl acrylate and stearyl acrylate; and methacylic acid alkyl esters such as methyl methacrylate, ethyl methacrylate, n-propyl methacrylate,
  • (meth) acrylic acid ester monomers having an alkyl group with 2 to 4 carbon atoms are preferable and ethyl(meth)acrylate and butyl(meth)acrylate are more preferable because they are flexible and have a low glass transition temperature and extremely low solubility to an electrolyte in the case of a homopolymer.
  • the glass transition temperature is not particularly limited as long as it is 80 degrees C or lower and can be suitably selected to suit to a particular application. It is preferably 40 degrees C or lower and more preferably 15 degrees C or lower. A polymer with a glass transition temperature of the upper limit of the range specified above or lower than that forms a flexible electrode mixture layer or solid electrolyte layer, thereby enhancing the resistance to peeling.
  • the polymer's glass transition temperature can be adjusted by changing the type and/or content of a (meth)acrylic acid alkyl ester or changing the type and/or ratio of the other monomers in a monomer composition for use in preparing the polymer.
  • the polymer's glass transition temperature can be measured according to JIS K7121 format.
  • the liquid mixture of the polymer and the solvent mentioned above in which the concentration of the polymer is 10 percent by mass has 50 mPa ⁇ s or less at 25 degrees C at 100 rotation per minute (rpm).
  • the solvent is contained in the liquid composition together with the polymer. This solvent is described later.
  • a liquid mixture with a viscosity of 50 mPa ⁇ s or lower sufficiently increases the solid content concentration of the liquid composition in preparing the liquid composition.
  • the viscosity of the liquid mixture can be adjusted by changing the number average molecular weight of the polymer or changing the amount of a cross-linkable monomer in a monomer composition for use in preparing the polymer.
  • the solid content concentration of a liquid composition refers to the mass percentage of the mass of the components other than the solvent to the entire mass of the liquid composition.
  • the components other than the solvent are free of mass decrease at 120 degrees C in a vacuum environment and include visco-elastic bodies such as dispersants in addition to the ion conductive materials, which are described later.
  • the viscosity in the present specification is measured at 25 degrees C.
  • the method of measuring the viscosity of the liquid mixture and liquid composition mentioned above is not particularly limited and can be suitably selected to suit to a particular application.
  • One way of measuring is according to the JIS Z 8803 format.
  • the device for this measuring is not particularly limited and can be suitably selected to suit to a particular application.
  • One of such devices is a TV25 type viscometer, cone and plate viscometer, manufactured by TOKI SANGYO CO., LTD.
  • the polymer is added to the liquid composition in the range of concentration by mass in which the polymer is dissolved in the solvent.
  • the content of the polymer in the liquid composition is within this range, the viscosity of the liquid composition is relatively likely to decrease and the liquid composition has excellent storage stability and re-dispersibility because the polymer particles remaining undissolved in the liquid composition do not bind with pigments such as ion conductive materials.
  • the content or proportion of the polymer in the liquid composition is preferably, 10 percent by mass or less, more preferably 5 percent by mass or less, furthermore preferably 3 percent by mass or less, and preferably 1 percent by mass or greater to the ion conductive material.
  • a liquid composition obtained has a sufficiently high solid content concentration and an electrode mixture layer or solid electrolyte layer obtained has sufficiently high resistance to peeling.
  • the ion conductive material in the present disclosure is not particularly limited and can be suitably selected to suit to a particular application. It includes, but is not limited to, a positive electrode active material, a negative electrode active material, and a solid electrolyte. These may be used alone or in a combination of two or more thereof.
  • the positive electrode active material is not particularly limited and can be suitably selected to suit to a particular application as long as it can receive or release an alkali metal ion.
  • One of the materials is an alkali metal-containing transition metal compound.
  • the alkali metal-containing transition metal compound is not particularly limited and can be suitably selected to suit to a particular application. It includes a lithium-containing transition metal compound such as a composite oxide containing lithium and one or more elements selected from the group consisting of cobalt, manganese, nickel, chromium, iron, and vanadium
  • lithium-containing transition metal compound examples include, but are not limited to, positive electrode active materials such as a lithium-containing cobalt oxide (LiCoO 2 ), lithium manganate (LiMn 2 O 4 ), a lithium-containing nickel oxide (LiNiO 2 ), a lithium-containing composite oxide of Co-Ni-Mn (Li (CoMnNi)O 2 ), a lithium-containing composite oxide of Ni-Mn-Al, a lithium-containing composite oxide of Ni-Co-Al, an olivine-type lithium iron-phosphate (LiFePO 4 ), an olivine-type lithium manganese-phosphate (LiMnPO 4 ), a Li 2 MnO 3 -LiNiO 2 based solid solution, a lithium-excess spinel compound represented by Lii + x Mn 2-x O 4 (0 ⁇ X ⁇ 2), Li[Ni 0.17 Li 0.2 Co 0.07 Mn 0.56 ]O 2 , and LiNi 0 5
  • the negative electrode active material is not particularly limited and can be suitably selected to suit to a particular application as long as it can receive or release an alkali metal ion.
  • One example of the negative electrode active materials is a carbon material containing graphite having a graphite crystal structure.
  • the carbon material include, but are not limited to, natural graphite, artificial graphite, non-graphitizable carbon (hard carbon), and graphitizable carbon (soft carbon).
  • the negative electrode active material other than the carbon material includes, but are not limited to, lithium titanate and titanium oxide.
  • the negative electrode active material such as silicone, tin, alloys of silicone, alloys of tin, silicon oxide, silicon nitride, and tin oxide in terms of energy density.
  • the maximum particle diameter of the active material in the present disclosure is not particularly limited and can be suitably selected to suit to a particular application unless it impairs the effects of the present disclosure.
  • the maximum particle diameter is smaller than the nozzle diameter of an inkjet head. It is preferably sufficiently smaller than the nozzle diameter of the inkjet head to enhance inkjet discharging ability.
  • the ratio of the maximum particle diameter of the active material contained in a liquid composition to the nozzle diameter of an inkjet head is preferably 0.8 or less, more preferably 0.6 or less, and furthermore preferably 0.5 or less. The discharging stability of the liquid composition ameliorates when the maximum particle diameter is within this range.
  • the nozzle diameter is 40 ⁇ m so that the maximum particle diameter of the active material contained in a liquid composition is preferably 32 ⁇ m or less, more preferably 24 ⁇ m or less, and furthermore preferably 20 ⁇ m or less.
  • the maximum particle diameter represents the diameter of the maximum distribution value in the particle size distribution of the active material in the liquid composition measured.
  • the method of measuring the maximum particle diameter of the active material is not particularly limited and can be suitably selected to suit to a particular application.
  • One way of measuring is according to the ISO 13320:2009 regulation.
  • the device for this measuring is not particularly limited and can be suitably selected to suit to a particular application. It includes a particle size analyzer utilizing laser diffraction, Mastersizer 3000, manufactured by Malvern Panalytical Ltd.
  • the modal diameter of the active material in the present disclosure is not particularly limited and can be suitably selected to suit to a particular application unless it has an adverse impact on the effects of the present disclosure. It is preferably from 0.5 to 10 ⁇ m and more preferably from 3 to 10 ⁇ m or less. Defective discharging using an active material with a modal diameter of from 0.5 to 10 ⁇ m is unlikely to occur when a liquid composition is discharged by a liquid discharging method. An active material's modal diameter of from 3 to 10 ⁇ m enhances the electrical properties of an electrode mixture layer. The modal diameter represents the diameter of the local maximum distribution value in the particle size distribution of the active material in the liquid composition measured.
  • the method of measuring the active material's modal diameter is not particularly limited and can be suitably selected to suit to a particular application.
  • One way of measuring is according to the ISO 13320:2009 regulation.
  • the device for this measuring is not particularly limited and can be suitably selected to suit to a particular application. It includes a particle size analyzer utilizing laser diffraction, Mastersizer 3000, manufactured by Malvern Panalytical Ltd.
  • the solid electrolyte is not particularly limited as long as it is ion conductive with an electron insulating property.
  • a solid electrolyte sulfide containing sulfur in its composition formula or a solid electrolyte oxide containing oxygen as the sole anion is preferable in terms of ion conductivity.
  • a solid electrolyte sulfide containing sulfur is more preferable to form a good interface in forming the interface between the ion conductive materials.
  • the inorganic solid electrolyte sulfide contains a sulfur atom (S) preferably with ion conductivity of a metal belonging to Group 1 or 2 of the periodic table and electron insulating properties.
  • S sulfur atom
  • the inorganic solid electrolyte sulfide preferably contains elements of at least Li, S, and P and has lithium ion conductivity. It can optionally contain elements other than Li, S, and P depending on a particular application.
  • composition Formula 1 One of such lithium ion conductive inorganic solid electrolytes satisfying Composition Formula 1 is as follows. L a1 M b1 P c1 S d1 A e1 Composition Formula 1
  • L represents an element selected from the group of Li, Na, K, and Ca. Of these, Li is preferable.
  • M represents an element selected from the group of B, Zn, Sn, Si, Cu, Ga, Sb, Al, Ge, and Y.
  • A represents an element selected from the group of I, Br, Cl, and F.
  • a1 to e1 represent the ratio of each composition. The ratio of a1:b1:c1:d1:e1 satisfies 1-12:0-5:1:2-12:0-10
  • the compositional ratio of each element can be adjusted by changing the ratio of raw materials mixed in manufacturing an inorganic solid electrolyte sulfide.
  • the inorganic solid electrolyte sulfide can be amorphous (glass), crystal (glass-ceramic), or partially crystal. It is possible to use Li-P-S based glass containing Li, P, and S and Li-P-S based glass ceramics containing Li, P, and S, for example.
  • the inorganic solid electrolyte sulfide can be manufactured by reacting at least two of the materials of lithium sulfide (Li 2 S), phosphrous sulfide (e.g., phosphorus pentasulfide, P 2 S 5 ), elemental phosphorous, elemental sulfur, sodium sulfide, hydrogen sulfide, lithium halaide (e.g., LiI, LiBr, LiCl), and sulfides of the element represented by M above (e.g., SiS 2 , SnS, and GeS 2 ).
  • Li 2 S lithium sulfide
  • phosphrous sulfide e.g., phosphorus pentasulfide, P 2 S 5
  • elemental phosphorous e.g., elemental sulfur
  • sodium sulfide e.g., sodium sulfide
  • hydrogen sulfide e.g., LiI, LiBr, LiC
  • the molar ratio of Li 2 S to P 2 S 5 in Li-P-S based glass and Li-P-S based glass ceramics is preferably from 60:40 to 90:10 and more preferably from 68:32 to 78:22. Within this range, lithium ion conductivity increases.
  • the lithium ion conductivity is preferably 1 ⁇ 10 -4 S/cm or greater and more preferably 1 ⁇ 10 -3 S/cm or greater. There is no maximum for this conductivity but practically 5 ⁇ 10 -1 S/cm or less.
  • Li 2 S-P 2 S 5 Li 2 S-P 2 S 5 , Li 2 S-P 2 S 5 -LiCl, Li 2 S-P 2 S 5 -H 2 S, Li 2 S-P 2 S 5 -H 2 S-LiCl, Li 2 S-LiI-P 2 S 5 , LizS-LiI-LizO-PzSs, Li 2 S-LiBr-P 2 S 5 , Li 2 S-Li 2 O-P 2 S 5 , Li 2 S-Li 3 PO 4 -P 2 S 5 , Li 2 S-P 2 S 5 -P 2 O 5 , Li 2 SP 2 S 5 -SiS 2 , Li 2 S-P 2 S 5 -SiS 2 -LiCl, Li 2 S-P 2 S 5 -SnS, Li 2 S-P 2 S 5 -Al 2 S 3 , Li 2 S-GeS 2 ,
  • the mixing ratio of each material is not limit for the mixing ratio of each material.
  • One way of synthesizing an inorganic solid electrolyte sulfide using such raw material compositions is an amorphous sizing method.
  • the amorphous sizing method includes a mechanical milling method, solution method, and melt extraction. These methods can be executed at room temperature, thereby simplifying the manufacturing processes.
  • the inorganic solid electrolyte oxide contains an oxygen atom (O) preferably with ion conductivity of a metal belonging to Group 1 or 2 of the periodic table and electron insulating properties.
  • Li 3 PO 4 lithium phosphate
  • LiPON obtained by partially substituting oxygens of lithium phosphate with nitrogens
  • LiPOD1 LiPOD1
  • D1 represents at least one of Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zr, Nb, Mo, Ru, Ag, Ta, W, Pt, and Au.
  • LiA1ON, where A1 is at least one of Si, B, Ge, Al, C, and Ga can also be preferably used.
  • the maximum particle diameter of the solid electrolyte in the present disclosure is not particularly limited and can be suitably selected to suit to a particular application unless it impairs the effects of the present disclosure.
  • the maximum particle diameter is preferably smaller than the nozzle diameter of an inkjet head and preferably sufficiently smaller than the nozzle diameter of the inkjet head to enhance inkjet discharging ability.
  • the ratio of the maximum particle diameter of the solid electrolyte contained in a liquid composition to the nozzle diameter of an inkjet head is preferably 0.8 or less, more preferably 0.6 or less, and furthermore preferably 0.5 or less.
  • the liquid composition's discharging stability ameliorates when the maximum particle diameter is within this range.
  • the nozzle diameter is 40 ⁇ m so that the maximum particle diameter of the active material contained in a liquid composition is preferably 32 ⁇ m or less, more preferably 24 ⁇ m or less, and furthermore preferably 20 ⁇ m or less.
  • the maximum particle diameter represents the maximal diameter in the particle size distribution of the solid electrolyte in the liquid composition measured.
  • the method of measuring the solid electrolyte's maximum particle diameter is not particularly limited and can be suitably selected to suit to a particular application.
  • One way of measuring is the same as the method of measuring the active material's maximum particle diameter.
  • the modal diameter of the solid electrolyte in the present disclosure is not particularly limited and can be suitably selected to suit to a particular application unless it adversely impacts the effects of the present disclosure. It is preferably from 0.1 to 10 ⁇ m and more preferably from 0.5 to 3 ⁇ m or less. Defective discharging using a solid electrolyte with a modal diameter of from 0.1 to 10 ⁇ m is unlikely to occur when a liquid composition is discharged by a liquid discharging method.
  • the modal diameter represents the diameter of the local maximum distribution value in the particle size distribution of the solid electrolyte in the liquid composition measured.
  • the method of measuring the solid electrolyte's modal diameter is not particularly limited and can be suitably selected to suit to a particular application.
  • One way of measuring is the same as the method of measuring the active material's modal diameter.
  • a dispersant disperses an ion conductive material and/or conductive assistant.
  • Some of the dispersants disperses both an ion conductive material and conductive assistant.
  • Such a dispersant corresponds to a dispersant for ion conductive material and a dispersant for conductive assistant.
  • the dispersant for ion conductive material in the present disclosure is not particularly limited as long as it does not react with the ion conductive material and can disperse the ion conductive material.
  • a dispersant with an ionic absorption group is preferable to enhance the dispersibility.
  • As the dispersant for ion conductive material a known or procured dispersant can be used.
  • Examples include, but are not limited to, polymeric dispersants such as polyethylene-based dispersants, polyethylene oxide-based dispersants, polypropylene oxide-based dispersants, polycarboxylic acid-based dispersants, naphthalenesulfonic acid-formalin condensation-based dispersants, polyethylene glycol-based dispersants, polycarboxylic acid partial alkyl ester-based dispersants, polyether-based dispersants, and polyalkylene polyamine-based dispersants; low-molecular dispersants such as alkylsulfonic acid-based dispersants, quaternary ammonium higher alcohol alkylene oxide-based dispersants, polyhydric alcohol ester-based dispersants, and alkylpolyamine-based dispersants; and inorganic dispersants such as polyphosphate dispersants. These can be used alone or in combination.
  • polymeric dispersants such as polyethylene-based dispersants, polyethylene oxide-based dispersants, polypropylene oxide-based dis
  • the content or proportion of the dispersant for ion conductive material in the liquid composition is preferably, 5 percent by mass or less, more preferably 3 percent by mass or less, furthermore preferably 1 percent by mass or less, and preferably 0.1 percent by mass or greater to the ion conductive material.
  • the ion conductive material is stably dispersed without impairing its surface function within this preferable range.
  • the dispersant for conductive assistant is not particularly limited as long as it does not react with a conductive assistant and can disperse the conductive assistant.
  • a known or procured dispersant can be used.
  • the same dispersant as that for ion conductive material can be used.
  • the content or proportion of the dispersant for conductive assistant in the liquid composition is preferably, 100 percent by mass or less, more preferably 50 percent by mass or less, furthermore preferably 30 percent by mass or less, and preferably 15 percent by mass or greater to the conductive assistant.
  • the conductive assistant is stably dispersed without affecting adversely its surface function within this preferable range. If a dispersant for a conductive assistant can adsorb an ion conductive material, the dispersant's isolated portion adsorbs the ion conductive material, thereby inhibiting impairing the surface function of the ion conductive material.
  • the solvent in the present disclosure is not particularly limited as long as it can dissolve the polymer mentioned above and can be suitably selected to suit to a particular application.
  • ketones such as acetone, methyl ethyl ketone, and cyclohexanone
  • esters such as ethyl acetate, butyl acetate, methyl butyrate, ethyl butyrate, butyl butyrate, methyl hexanoate, ethyl hexanoate, methyl heptanoate, ethyl heptanoate, ethyl isobutyrate, isobutyl isobutyrate, isoamyl isobutyrate, ethyl isovalerate, and isobutyl isovalerate; ethers such as diethyl ether, dioxane, and tetrahydrofuran; amide polar organic solvents such as N, N-dimethylformamide and N-methyl-2-pyrrolidone (NMP); aromatic hydrocarbons such as toluene, xylene, and
  • water-insoluble solvents such as methyl butyrate, ethyl butyrate, butyl butyrate, methyl hexanoate, ethyl hexanoate, methyl heptanoate, ethyl heptanoate, ethyl isobutyrate, isobutyl isobutyrate, isoamyl isobutyrate, ethyl isovalerate, and isobutyl isovalerate, and water-soluble solvents such as N-methyl-2-pyrrolidone, ⁇ -butyrolactone, dimethyl sulfoxide, and N,N-dimethylformamide are preferable to lower the viscosity of the liquid composition, thus enhancing the dispersibility thereof.
  • carboxylic acid esters such as methyl butyrate, methyl valerate, methyl hexanoate, methyl heptanoate, methyl decanoate, ethyl butyrate, ethyl valerate, ethyl hexanoate, ethyl heptanoate, ethyl decanoate, butyl butyrate, ethyl isobutyrate, isobutyl isobutyrate, isoamyl isobutyrate, ethyl isovalerate, isobutyl isovalerate, and isoamyl isovalerate are preferable to lower the viscosity of a liquid composition with a high solid content concentration, thus enhancing the dispersibility thereof
  • the other optional components are not particularly limited and can be suitably selected to suit to a particular application unless it affects adversely the effects of the present disclosure. It includes, for example, a conductive assistant.
  • Examples of the conductive assistant include, but are not limited to, carbon black produced by a method such as a furnace method, an acetylene method, and a gasification method, and carbon materials such as carbon nanofibers, carbon nanotubes, graphene, and graphite particles.
  • Conductive assistants other than the carbon materials include, but are not limited to, metal particles and metal fiber of aluminum.
  • the conductive assistant may be combined with an active material in advance.
  • the upper limit of the mass ratio of the conductive assistant to an active material is preferably 10 percent by mass or less, more preferably 5 percent by mass or less, and furthermore preferably 3 percent by mass or less, and the lower limit is preferably 1 percent by mass or more.
  • a mass ratio of the conductive additive to an active material satisfying the lower limit value enhances the conductivity of an obtained electrode mixture layer.
  • a mass ratio of the conductive additive to an active material satisfying the upper limit value enhances the energy density without impairing the conductivity of an obtained electrode mixture layer.
  • the liquid composition mentioned above preferably has a viscosity sufficient for a liquid discharging head to be able to discharge it. Specifically, it is preferably 200 mPa ⁇ s or less, more preferably 100 mPa ⁇ s, and furthermore 50 mPa ⁇ s or less. In addition, it is preferably 10 mPa ⁇ s or greater and more preferably 30 mPa ⁇ s or greater.
  • a liquid composition with a viscosity satisfying the lower limit mentioned above inhibits the flow of an applied liquid composition during drying. The film obtained is free of unevenness in thickness and locality regarding components.
  • the liquid composition's solid content concentration is preferably 20 percent by mass or greater, more preferably 60 percent by mass or greater, and furthermore preferably 65 percent by mass or greater.
  • a liquid composition with a viscosity satisfying the upper limit mentioned above is likely to demonstrate thixotropy, which inhibits flowing of the applied liquid composition during drying so that the film obtained has a uniform thickness and is free of unevenness regarding the components.
  • the liquid composition containing an active material as an ion conductive material has a viscosity of from greater than 20 mPa ⁇ s to less than 200 mPa ⁇ s.
  • the liquid composition containing an active material as an ion conductive material preferably has a solid content concentration of 60 percent by mass or greater.
  • the liquid composition containing a solid electrolyte as an ion conductive material has a viscosity of 20 mPa ⁇ s or less.
  • the liquid composition containing a solid electrolyte as an ion conductive material preferably has a solid content concentration of 20 percent by mass or greater and more preferably 30 percent by mass or greater.
  • the liquid composition can be produced by dissolving or dispersing each of the components mentioned above in the solvent mentioned above.
  • the liquid composition can be prepared by mixing each of the components mentioned above with the solvent using a mixer, such as a ball mill, a sand mill, a bead mill, a pigment disperser, a grinder, an ultrasonic disperser, a homogenizer, a planetary mixer, or a filmix.
  • a mixer such as a ball mill, a sand mill, a bead mill, a pigment disperser, a grinder, an ultrasonic disperser, a homogenizer, a planetary mixer, or a filmix.
  • the application of the liquid composition is not particularly limited and can be suitably selected to suit to a particular application.
  • the liquid composition may be suitably used as a material for forming a layer containing an ion conductive material such as a solid electrolyte layer such as an electrode mixture layer and a solid electrolyte layer in an electrochemical device.
  • a liquid composition containing at least the positive electrode active material or the negative electrode mentioned above as an ion conductive material can be used as a liquid composition for forming an electrode of a secondary battery.
  • a liquid composition containing at least the solid electrolyte mentioned above as an ion conductive material can be used as a liquid composition for forming a solid electrolyte layer of a secondary battery.
  • the liquid composition of the present embodiment can be suitably used as a liquid composition for inkjet discharging.
  • the electrode also referred to as an electrode for a secondary battery related to the present embodiment includes an electrode substrate and an electrode mixture layer formed on the electrode.
  • the electrode mixture layer is formed with the liquid composition of the present embodiment.
  • the electrode mixture layer contains at least the ion conductive material, the dispersant for the ion conductive material, and the polymer mentioned above.
  • Each component contained in the electrode mixture layer is the same as that contained in the liquid composition mentioned above.
  • the suitable ratio of each component is the same as that of each component in the liquid composition.
  • the present embodiment's electrode uses the present embodiment's liquid composition, thereby forming an electrode mixture layer with a high resistance to peeling on a current collector.
  • Materials with electric conductivity and electrochemical resistance are used to constitute an electrode substrate.
  • Such materials for an electric substrate include, but are not limited to, iron, copper, aluminum, nickel, stainless steel, titanium, tantalum, gold, and platinum.
  • the materials mentioned above can be used alone or in combination at an arbitrary ratio.
  • the method of manufacturing the electrode of the present embodiment includes applying the liquid composition of the present embodiment to an electrode substrate and other optional processes.
  • the method of applying the liquid composition is not particularly limited.
  • liquid discharging methods such as an inkjet method, a spray coating method, and a dispenser method, spin coating, casting, MICROGRAVURE TM coating, gravure coating, bar coating, roll coating, wire bar coating, dip coating, slit coating, capillary coating, nozzle coating, gravure printing, screen printing, flexographic printing, offset printing, and reverse printing.
  • the inkjet method is particularly preferable.
  • a free-shaped electrode can be manufactured in a non-contact manner. This manufacturing method reduces the loss of the active material caused by punching in producing an electrode.
  • the liquid composition can be applied to one or both sides of a current collector.
  • the thickness of the liquid composition on a current collector after applying and before drying can be suitably adjusted according to the thickness of an electrode mixture layer obtained after drying.
  • the method of drying the liquid composition on a current collector is not particularly limited and any known method can be employed.
  • Specific examples include, but are not limited to, a method using warm air, heated wind, or low moisture wind, vacuum drying, a method using radiation of infra red and electron beams.
  • a laminate of a solid electrolyte layer and an electrode relating to the present embodiment includes an electrode and a solid electrolyte layer formed on the electrode.
  • the solid electrolyte layer is formed with the liquid composition of the present embodiment.
  • the solid electrolyte layer contains at least the ion conductive material, the dispersant for the ion conductive material, and the polymer.
  • Each component in the solid electrolyte layer is the same as that in the liquid composition mentioned above.
  • the suitable ratio of each component is the same as that of each component in the liquid composition.
  • the present embodiment's laminate uses the present embodiment's liquid composition, thereby forming a solid electrolyte layer with a high resistance to peeling on a current collector.
  • the solid electrolyte can be formed by the same method as the method of manufacturing an electrode as described above except for forming on an electrode.
  • the container of the present disclosure contains the liquid composition or liquid composition for inkjet discharging of the present disclosure.
  • the size, shape, and structure of the container is not particularly limited and they can be suitably selected to suit to a particular application.
  • the device for manufacturing a part of the electrochemical device of the present disclosure includes the container of the present disclosure, a discharging device for discharging the liquid composition accommodated in the container using an inkjet head or liquid discharging head, and other optional devices.
  • Manufacturing a part of the electrochemical device of the present disclosure includes discharging the liquid composition or liquid composition for inkjet discharging of the present disclosure using an inkjet head and other optional processes.
  • the electrochemical device's part has a variety depending on the type of ion conductive material used. Examples include, but are not limited to, an electrode mixture layer and a solid electrolyte layer.
  • the discharging device discharges the liquid composition or the liquid composition for inkjet discharging contained in the container using an inkjet head.
  • the discharging process executes discharging the liquid composition or the liquid composition for inkjet discharging using an inkjet head.
  • the liquid composition or the liquid composition for inkjet discharging is applied onto a target to form a liquid composition layer.
  • the target also referred to as the target for discharging, is not particularly limited and can be suitably selected to suit to a particular application as long as it is a target on which an ion conductive material containing layer is formed.
  • Examples include, but are not limited to, an electrode substrate, also referred to as a current collector, and an active material layer.
  • the other optional devices relating to the device for manufacturing an electrochemical device's part is not particularly limited and can be suitably selected to suit to a particular application unless it adversely impacts the effects of the present disclosure. It includes, for example, a heating device.
  • the other optional process relating to the method of manufacturing an electrochemical device's part is not particularly limited and can be suitably selected to suit to a particular application unless it has an adverse impact on the effects of the present disclosure. It includes, for example, heating.
  • the heating device heats the liquid composition or the liquid composition for inkjet discharging discharged with the discharging device.
  • the heating process executes heating the liquid composition or the liquid composition for inkjet discharging discharged in the discharging process.
  • the liquid composition layer can be dried by the heating.
  • FIG. 1 is a schematic diagram illustrating an example of the method of manufacturing an electrochemical device's part according to an embodiment of the present invention.
  • a liquid composition 12A is stored in a tank 307 of a liquid discharging device 300 and supplied from the tank 307 to a liquid discharging head 306 via a tube 308.
  • the number of the liquid discharging devices is not limited to one but can be two or more.
  • an electrode substrate 11 is disposed on a stage 310 and then the liquid discharging head 306 discharges liquid droplets of the liquid composition 12A to the electrode substrate 11. At this point, it is possible to move the stage 310 or the liquid discharging head 306.
  • the liquid composition 12A discharged forms an electrode mixture layer 12.
  • liquid discharging device 300 may optionally include a mechanism of capping the nozzle of the liquid discharging head 306 to prevent it from drying while the liquid discharging head is not discharging the liquid composition 12A.
  • FIG. 2 is a schematic diagram illustrating an example of the device 1000 for manufacturing an electrochemical device's part that executes the method of manufacturing a part of the electrochemical device of the present embodiment.
  • the device 1000 for manufacturing an electrochemical device's part illustrated in FIG. 2 manufactures a solid electrolyte layer or an electrode mixture layer using the liquid composition mentioned above.
  • the device 1000 for manufacturing an electrochemical device' part includes a discharging unit 10 for applying a liquid composition 7 to a print substrate 4 having a target for discharging to form a liquid composition layer and a heating unit 30 for heating the liquid composition layer to obtain an ion conductive material layer.
  • the device 1000 for manufacturing an electrochemical device's part includes a conveyor unit 5 that conveys the print substrate 4 in the sequence of the discharging unit 10 and the heating unit 30 at a preset speed.
  • the method of manufacturing the print substrate 4 having a target for discharging such as the electrode substrate or the active material mentioned above is not particularly limited.
  • the print substrate can be manufactured utilizing a known method.
  • the discharging unit 10 includes a print device 1a as an example of the application device that applies the liquid composition 7 onto the print substrate 4, a container 1b that contains the liquid composition 7, and a supply tube 1c that supplies the liquid composition 7 in the container 1b to the print device 1a.
  • the container 1b accommodates the liquid composition 7.
  • the discharging unit 10 discharges the liquid composition 7 from the print device 1a to apply the liquid composition 7 onto the print substrate 4 to form a thin film-like liquid composition layer.
  • the container 1b may be configured in an integrated manner with a device for manufacturing an electrochemical device's part. Alternatively, it can be configured removable from a device for manufacturing an electrochemical device's part. In addition, the container 1b may be configured to add the liquid composition 7 to a container integrated with a device for manufacturing an electrochemical device's part or a container detachable from a device for manufacturing an electrochemical device's part.
  • the container 1b and the supply tube 1c can be arbitrarily selected as long as the liquid composition 7 can be stably stored and supplied.
  • a heating unit 30 includes a heater 3a.
  • the heater 3a heats and dries a solvent remaining in the liquid composition layer to remove it. An ion conductive material containing layer is thus formed.
  • the heating unit 30 may remove the solvent under a reduced pressure.
  • the heater 3a is not particularly limited and can be suitably selected to suit to a particular application. It includes, but is not limited to, a substrate heater, an IR heater, a heated wind heater, and a combination thereof.
  • heating temperature and the heating time can be appropriately selected according to the boiling point of the solvent contained in the liquid composition 7 and the thickness of formed film.
  • FIG. 3 is a schematic diagram illustrating another example of the device 2000 for manufacturing an electrochemical device's part that executes the method of manufacturing a part of the electrochemical device of the present embodiment.
  • Aliquid discharging device 300' circulates a liquid composition in a liquid discharging head 306, a tank 307, and a tube 308 by adjusting a pump 3101 and valves 311 and 312.
  • the liquid discharging device 300' includes an external tank 313.
  • the liquid composition can be supplied to the tank 307 from the external tank 313 by adjusting the pump 3101 and the valves 311, 312, and 314 when the liquid composition in the tank 307 decreases.
  • the liquid composition is discharged to the target position on a target substrate using the device for manufacturing an electrochemical device's part.
  • the solid electrolyte layer or the electrode mixture layer as an example of the ion conductive material layer can be suitably used as a part constituting an electrochemical device.
  • the configuration other than the solid electrolyte layer or the electrode mixture layer is not particularly limited A known member, such as a positive electrode, a negative electrode, and a separator, can be used for the configuration.
  • FIG. 4 is a diagram illustrating an example of the method of manufacturing an electrode according to the present embodiment.
  • the method of manufacturing an electrode 100 includes sequentially discharging a liquid composition 12A onto the electrode substrate 11 using the liquid discharging device 300'.
  • the electrode substrate 11 prepared has a long and thin shape.
  • the electrode substrate 11 is wound around a tubular core.
  • a feeding roller 304 and a reeling roller 305 are disposed in order to form the electrode mixture layer 12 on the upper surface in FIG. 4 .
  • the feeding roller 304 and the reeling roller 305 rotate counterclockwise to convey the electrode substrate 11 from the right to left in FIG. 4 .
  • the liquid discharging head 306 disposed above the electrode substrate 11 between the feeding roller 304 and the reeling roller 305 discharges liquid droplets of the liquid composition 12A onto the electrode substrate 11 sequentially conveyed in the same manner as illustrated in FIG. 1 .
  • Two or more of the liquid discharging heads 306 can be positioned in the direction substantially parallel or perpendicular to the conveyance direction of the electrode substrate 11.
  • the electrode substrate 11 onto which the liquid droplets of the liquid composition 12A are discharged is conveyed to a heating mechanism 309 by the feeding roller 304 and the reeling roller 305.
  • the electrode mixture layer 12 is formed to obtain an electrode 100.
  • the electrode 100 is cut to a desired size by processing, such as punching.
  • the heating mechanisms 309 can be disposed either above or below the electrode substrate 11 or two or more of the heating mechanisms 309 may be disposed.
  • the heating mechanism 309 is not particularly limited unless it contacts the liquid composition 12A in a direct manner. It includes, but is not particularly limited to, a resistance heater, an infrared heater, and a fan heater. Two or more of the heating mechanism 309 can be disposed. A device for curing utilizing ultraviolet can be also disposed for polymerization.
  • the liquid composition 12A discharged to the electrode substrate 11 is preferably heated at the stage or with a heating mechanism other than the stage.
  • the heating mechanism 309 can be disposed either above or below the electrode substrate 11 or two or more of the heating mechanisms 309 may be disposed.
  • the heating temperature is not particularly limited.
  • the liquid composition 12A dries by heating, thereby forming an electrode mixture layer.
  • the tank 307 may supply ink from tanks 313A and 313B connected to tanks 307A and 307B, respectively.
  • the liquid discharging head 306 may include a head 306A and a head 306B.
  • FIGS. 6 and 7 are diagrams illustrating examples of the printing units employing a transfer method and an inkjet method as applying devices.
  • FIG. 6 is a diagram illustrating a printing unit using an intermediate transfer drum and
  • FIG. 7 is a diagram illustrating a printing unit using an endless intermediate belt.
  • a printing unit 400' illustrated in FIG. 6 transfers a liquid composition layer or ion conductive material containing layer to a substrate via an intermediate transfer member 4001 to form an ion conductive material containing layer on the substrate by inkjetting.
  • the printing unit 400' includes an inkjet unit 420, a transfer drum 4000, a pre-processing unit 4002, an absorption unit 4003, a heating unit 4004, and a cleaning unit 4005.
  • the inkjet unit 420 include a head module 422 holding multiple heads 401.
  • the heads 401 discharge a liquid composition to the intermediate transfer member 4001 supported by the transfer drum 4000 to form a liquid composition layer on the intermediate transfer member 4001.
  • Each of the heads 401 is a line head.
  • the nozzles thereof are disposed to cover the width of the maximal printing region of a usable substrate.
  • the heads 401 includes a nozzle surface on which the nozzles are formed.
  • the nozzle surface faces the surface of the intermediate transfer member 4001 with a tiny gap therebetween.
  • the intermediate transfer member 4001 is configured to move circularly on a circular orbit.
  • the heads 401 are thus radially positioned.
  • the transfer drum 4000 faces an impression cylinder 621, forming a transfer nip.
  • the pre-processing unit 4002 may apply a reaction liquid to the intermediate transfer member 4001 to increase the viscosity of a liquid composition before the heads 401 discharge the liquid composition.
  • the absorption unit 4003 absorbs the liquid composition from the liquid composition layer on the intermediate transfer member 4001 before transferring.
  • the heating unit 4004 heats the ink layer on the intermediate transfer member 4001 before transferring.
  • the liquid composition is dried by heating, forming an ion conductive material containing layer.
  • the organic solvent is removed, thereby enhancing the transferability to the substrate.
  • the cleaning unit 4005 cleans the surface of the intermediate transfer member 4001 after transferring and removes ink and impurities such as dusts remaining on the intermediate transfer member 4001.
  • the impression cylinder 621 is pressed against the intermediate transfer member 4001.
  • the liquid composition layer or ion conductive material containing layer on the intermediate transfer member 4001 is transferred to the substrate when the substrate passes the transfer nip between the impression cylinder 621 and the intermediate transfer member 4001.
  • the impression cylinder 621 can be configured to include at least one gripping mechanism for holding the front end of the substrate on its outer surface.
  • a printing unit 400" illustrated in FIG. 7 transfers a liquid composition layer or ion conductive material containing layer to a substrate via an intermediate transfer belt 4006 to form an ion conductive material containing layer on the substrate by inkjetting.
  • the printing unit 400 discharges liquid droplets of the liquid composition from the heads 401 of the inkjet unit 420 to form a liquid composition layer on the outer surface of the intermediate transfer belt 4006.
  • the heating unit 4007 dries the liquid composition layer formed on the intermediate transfer belt 4006 by heating, thereby forming film of an ion conductive material containing layer on the intermediate transfer belt 4006.
  • the filmed ion conductive material containing layer on the intermediate transfer belt 4006 is transferred to the substrate at the transfer nip formed between the intermediate transfer belt 4006 and a transfer roller 622.
  • a cleaning roller 4008 cleans the surface of the intermediate transfer belt 4006 after this transfer.
  • the intermediate transfer belt 4006 is stretched by a driving roller 4009a, a facing roller 4009b, multiple (four in this embodiment) shape maintaining rollers, 4009c, 4009d, 4009e, and 4009f, and multiple (four in this embodiment) supporting rollers 4009g.
  • the intermediate transfer belt 4006 moves in the direction indicated by the arrow in FIG. 7 .
  • the supporting rollers 4009g disposed facing the heads 401 maintain the tension of the intermediate transfer belt 4006 when the heads 401 discharge ink droplets.
  • FIG. 8 is a diagram illustrating an example of the negative electrode of the present embodiment.
  • a negative electrode 101 includes a negative electrode substrate 111 with a negative electrode material mixture layer 121 formed on one side of the negative electrode substrate 111.
  • the shape of the negative electrode 101 is not particularly limited and can be a planar plate, for example.
  • the negative electrode substrate 111 can be made of materials such as stainless steel, nickel, aluminum, and copper.
  • the negative electrode material mixture layer 121 can be formed on both sides of the negative electrode substrate 111.
  • the negative electrode can be manufactured by using a device for manufacturing an electrochemical device's part mentioned above.
  • FIG. 9 is a diagram illustrating an example of the positive electrode of the present embodiment.
  • the positive electrode 20 includes the positive electrode substrate 21 with a positive electrode material mixture layer 22 on one side of the positive electrode substrate 21.
  • the shape of the positive electrode 20 is not particularly limited and can be a planar plate, for example.
  • the positive electrode substrate 21 can be made of materials such as stainless steel, aluminum, titanium, and tantalum.
  • the positive electrode material mixture layer 22 can be formed on both sides of the positive electrode substrate 21.
  • the positive electrode can be manufactured by using a device for manufacturing an electrochemical device's part mentioned above.
  • the electrochemical device of the present disclosure includes a current collector and a layer containing at least an ion conductive material, a dispersant for ion conductive material, and a polymer on the current collector.
  • the electrochemical device may contain other optional configurations.
  • the layer containing at least an ion conductive material, a dispersant for ion conductive material, and a polymer can be formed on a current collector directly or with another layer therebetween.
  • the electrochemical device includes a positive electrode, a negative electrode, and a solid electrolyte layer or a liquid electrolyte with optional members, such as a separator and an exterior.
  • the electrochemical device contains the liquid composition of the present disclosure as at least one of the positive electrode, the negative electrode, and the solid electrolyte layer. No separator is necessary when a solid electrolyte or a gel electrolyte is used.
  • the current collector is the same as those mentioned above as the electrode substrate.
  • the ion conductive material, the dispersant for ion conductive material, and the polymer are the same as those for the ion conductive material, the dispersant for ion conductive material in the liquid composition.
  • the electrochemical device of the present disclosure preferably uses the electrode of the present embodiment as a positive electrode.
  • a lithium ion secondary battery is described but the present invention is not limited thereto.
  • the electrode other than the electrode mentioned above of the present embodiment that can be applied to the secondary battery mentioned above is not particularly limited. It includes a known electrode for use in manufacturing a secondary battery. An electrode formed of an electrode mixture layer on a current collector utilizing a known manufacturing method is one such example.
  • the electrolyte other than the solid electrolyte layer mentioned above of the present embodiment that can be applied to the secondary battery mentioned above is not particularly limited. It includes a known solid or liquid electrolyte for use in manufacturing a secondary battery.
  • liquid electrolyte an organic liquid electrolyte in which a supporting electrolyte is dissolved in an organic solvent is used.
  • a lithium salt is used as a supporting electrolyte for a lithium ion secondary battery, for example.
  • lithium salts include, but are not limited to, LiPF 6 , LiAsF 6 , LiBF 4 , LiSbF 6 , LiAlCl 4 , LiClO 4 , CF 3 SO 3 Li, C 4 F 9 SO 3 Li, CF 3 COOLi, (CF 3 CO) 2 NLi,(CF 3 SO 2 ) 2 NLi, and (C 2 F 5 SO 2 )NLi.
  • LiPF 6 , LiClO 4 , and CF 3 SO 3 Li are preferable and LiPF 6 is more preferable because these are readily dissolved in a solvent, exhibiting high degree of dissociation.
  • These electrolytes can be used alone or in combination at any ratio.
  • a high degree of dissociation in a supporting electrolyte is likely to achieve a high lithium ion conductivity. In other words, the lithium ion conductivity depends on the type of supporting electrolyte.
  • the organic solvent for use in a liquid electrolyte is not particularly limited as long as it dissolves a supporting electrolyte.
  • Specific examples include, but are not limited to, carbonates such as dimethyl carbonate (DMC), ethylene carbonate (EC), diethyl carbonate (DEC), propylene carbonate (PC), butylene carbonate (BC) and ethyl methyl carbonate (EMC), esters such as ⁇ -butyrolactone and methyl formate, ethers such as 1,2-dimethoxyethane and tetrahydrofuran, sulfur-containing compounds such as sulfolane and dimethyl sulfoxide.
  • a liquid mixture of these solvents can be also used.
  • carbonates are preferable and a mixture of an ethylene carbonate and a diethyl carbonate are more preferable because they have a high dielectric constant and a large and stable voltage region.
  • concentration of the electrolyte in a liquid electrolyte can be suitably changed to suit to a particular application.
  • a known additive, such as vinylene carbonate can be added to a liquid electrolyte.
  • the separator is not particularly limited.
  • Specific examples include, but are not limited to, but are not limited to, paper such as kraft paper, vinylon mixed paper, and synthetic pulp mixed paper, cellophane, polyolefin nonwoven fabric such as polyethylene graft membrane and polypropylene melt blown nonwoven fabric, polyamide nonwoven fabric, and glass fiber nonwoven fabric, and micropore membrane.
  • paper such as kraft paper, vinylon mixed paper, and synthetic pulp mixed paper
  • cellophane cellophane
  • polyolefin nonwoven fabric such as polyethylene graft membrane and polypropylene melt blown nonwoven fabric
  • polyamide nonwoven fabric polyamide nonwoven fabric
  • glass fiber nonwoven fabric and micropore membrane.
  • the exterior is not particularly limited as long as it can seal an electrode, an electrolyte, and a separator or a solid electrolyte or a gel electrolyte.
  • the device for manufacturing the electrochemical device of the present disclosure includes a unit for manufacturing an electrochemical device's part with the device for manufacturing an electrochemical device's part of the present disclosure and other optional configurations.
  • the method of manufacturing the electrochemical device of the present disclosure includes manufacturing an electrochemical device's part by the method of manufacturing an electrochemical device's part of the present disclosure and other optional processes.
  • the device for manufacturing the electrochemical device of the present embodiment and the method of manufacturing the electrochemical device of the present embodiment may suitably employ a known unit or process in addition to the unit for manufacturing an electrochemical device's part mentioned above and the process of manufacturing an electrochemical device's part.
  • One way of manufacturing the electrochemical device of the present embodiment is: to superpose a positive electrode and a negative electrode with a separator therebetween, optionally followed by winding or folding in accordance with the shape of a battery; then place the product in a battery container; and fill the battery container with a liquid electrolyte; and seal the container.
  • FIG. 10 is a diagram illustrating an example of the electrode device for use in the electrochemical device relating to the present embodiment.
  • a negative electrode 15 and a positive electrode 25 are laminated via a separator 30B.
  • the positive electrode 25 is disposed on both sides of the negative electrode 15.
  • a lead wire 41 is connected to the negative electrode substrate 11B.
  • a lead wire 42 is connected to the positive electrode substrate 21.
  • the separator 30B is replaced with a solid electrolyte or a gel electrolyte if a solid electrochemical device is used.
  • the negative electrode 15 includes the negative substrate 11 with negative electrode material mixture layers 12 formed on both sides.
  • the positive electrode 25 includes the positive electrode substrate 21 with positive electrode material mixture layers 22 formed on both sides.
  • the number of the lamination of the negative electrodes 15 and the positive electrodes 25 of the electrode device 40 is not particularly limited. In addition, the number of the negative electrode 15 and the positive electrode 25 of the electrode device 40 can be the same or different.
  • FIG. 11 is a diagram illustrating an example of the electrochemical device relating to the present embodiment.
  • an electrolyte layer 51 is formed by injecting an aqueous solution of electrolyte or a non-aqueous electrolyte into the electrode device 40.
  • An exterior 52 seals the electrode device 40.
  • the lead wires 41 and 42 are led out to the outside of the exterior 52.
  • the separator 30B is replaced with a solid electrolyte or a gel electrolyte if the electrochemical device 1 is a solid electrolyte device.
  • the shape of the electrochemical device 1 is not particularly limited.
  • Examples include, but are not limited to, a laminate type, a cylinder type in which a sheet electrode and a separator are formed in a spiral shape, a cylinder type having an inside-out structure in which a pellet electrode and a separator are combined, and a coin type in which a pellet electrode and a separator are stacked.
  • the application of the electrochemical device is not particularly limited.
  • Examples include, but are not limited to: mobile objects such as vehicles; and electric devices, such as mobile phones, notebook computers, pen-input personal computers, mobile personal computers, electronic book players, cellular phones, portable facsimiles, portable copiers, portable printers, headphone stereos, video movies, liquid crystal televisions, handy cleaners, portable compact discs (CDs), minidiscs, transceivers, electronic notebooks, calculators, memory cards, portable tape recorders, radios, backup power supplies, motors, lighting devices, toys, game machines, watches, strobes, and cameras.
  • vehicles and electric devices are particularly preferable.
  • the mobile objects include, but are not limited to, ordinary vehicles, heavy special cars, small special vehicles, trucks, heavy motorcycles, and ordinary motorcycles.
  • FIG. 12 is a schematic diagram illustrating an example of a mobile object carried in an all-solid-state battery as an example of the electrochemical device of the present embodiment.
  • a mobile object 550 is an electric vehicle, for example.
  • the mobile object 550 includes a motor 551, an electrochemical device 552, and wheels 553 as an example of transportation device.
  • the electrochemical device 552 is the electrochemical device of the present embodiment mentioned above.
  • the electrochemical device 552 drives a motor 551 by supplying electricity to the motor 551.
  • the motor 551 driven can drive the wheels 553, thereby making the mobile object 550 travel.
  • the mobile object safely travels by the electricity from the electrochemical device with a high resistance to peeling.
  • the mobile object 550 can be applied not only to an electric vehicle but to a plug-in hybrid vehicle, a hybrid electric vehicle, and a locomotive or motorcycle that can travel on the combination of a diesel engine and an electrochemical device.
  • the mobile object can be a transport robot used in a factory, which can travel on an electrochemical device alone or a combination of an electrochemical device and an engine.
  • the mobile object includes a partially-movable object like an assembly robot in a factory's production line which has an arm performing on an electrochemical device or a combination of an engine and an electrochemical device.
  • the viscosity of the liquid composition and the viscosity of the liquid mixture of a polymer and a solvent in which the concentration of the polymer is 10 percent by mass were measured in the following manner.
  • the thixotropy index of the liquid composition was evaluated in the following manner.
  • the solid content concentration of a liquid composition was calculated in the following manner. The variation in the film thickness and the resistance to peeling of the electrode mixture layers or solid electrolyte layers obtained using the liquid composition were measured and evaluated in the following manner.
  • the viscosity of the liquid mixture or the liquid composition obtained was measured at 100 rpm and a room temperature of 25 degrees C using a TV25 viscometer, cone and plate viscometer, manufactured by TOKI SANGYO CO., LTD.
  • the solvent in the liquid mixture refers to the solvent in the liquid composition.
  • the viscosity of the liquid composition obtained was measured at 100 rpm and 10 rpm at a room temperature of 25 degrees C using a TV25 viscometer, cone and plate viscometer, manufactured by TOKI SANGYO CO., LTD.
  • the thixotropy index (TI) was calculated based on the ratio and the relationship below, followed by evaluating according to the following criteria.
  • the solid content concentration of a liquid composition was calculated according to the following relationship.
  • the entire solid content refers to the component free of mass decrease at 120 degrees C in a vacuum environment.
  • Solid content concentration entire of solid content in parts by mass / entire of solid content in parts by mass + solvent in parts by mass ⁇ 100 percent .
  • the positive electrodes for a secondary battery or the solid electrolyte layers or positive electrode laminates for a secondary battery manufactured in Examples and Comparative Examples were cut out to rectangles with a length of 50 mm and a width of 30 mm as test pieces.
  • the film thickness of these test pieces was measured at six points in total spaced 15 mm apart from each other in the major axis direction and the minor axis direction.
  • the positive electrode mixture layer's thickness or solid electrolyte layer's thickness is obtained by subtracting the substrate's thickness from the measuring values.
  • an aluminum foil substrate is used and, for the solid electrolyte or positive electrode laminate, a positive electrode for a secondary battery.
  • the thickness measurements of the positive electrode mixture layer or solid electrolyte layer at the six points were averaged and the standard deviation thereof was calculated.
  • the evaluation criteria are as follows. A small ratio of the standard deviation to the average thickness reads closer to a uniform application.
  • the positive electrodes for a secondary battery or the solid electrolyte layers or positive electrode laminates for a secondary battery manufactured in Examples and Comparative Examples were cut out to rectangles with a length of 50 mm and a width of 30 mm as test pieces.
  • a scotch tape conforming to JIS Z1522 format was attached to the surface of the test piece with the positive electrode mixture layer or solid electrolyte layer up.
  • the stress was measured when one end of the current collector was pulled and peeled at a tensile speed of 30 mm/minute in the perpendicular direction. This stress measured was defined as the resistance to peeling and evaluated according to the following criteria.
  • the test pieces graded from A to C are allowable. A large resistance value reads excellent attachability.
  • a nickel-based positive electrode active material (hereinafter also referred to as NCM, manufactured by TOSHIMA Manufacturing Co., Ltd.), an acid dispersant (SC-0708A, 1 percent by mass to the active material, manufactured by NOF CORPORATION) as a dispersant for ion conductive material, and PBMA (3 percent by mass to the active material) were mixed in a solvent (anisole) at a mass ratio to achieve a solid content concentration of 55 percent by mass based on the quantity calculated for preparation.
  • the viscosity of the liquid composition was measured according to the method described above. The evaluation results are shown in Table 1.
  • the liquid composition obtained according to the mentioned above was applied with an applicator to an aluminum foil as a current collector with a thickness of 20 ⁇ m to obtain a positive electrode mixture layer with an average film thickness of 80 ⁇ m.
  • the liquid composition on the aluminum foil was dried in an oven at 120 degrees C to obtain a positive electrode for a secondary battery with a positive electrode on the current collector.
  • the film thickness's variation and the resistance to peeling of the positive electrode for a secondary battery were evaluated according to the manner described above. The evaluation results are shown in Table 1.
  • Example 1 The same operations, measuring, and evaluation as those in Example 1 were conducted except that the polymer was changed to a copolymer of poly(butylmethacrylate-methyl methacrylate) (hereinafter, also referred to as P(BMA-MMA), manufactured by Sigma-Aldrich Co. LLC.). The results are shown in Table 1.
  • P(BMA-MMA) poly(butylmethacrylate-methyl methacrylate)
  • Example 1 The same operations, measuring, and evaluation as those in Example 1 were conducted except that the polymer was changed to polyethylmethacrylate (hereinafter, also referred to as PEMA), manufactured by Sigma-Aldrich Co. LLC.). The results are shown in Table 1.
  • PEMA polyethylmethacrylate
  • Example 2 The same operations, measuring, and evaluation as those in Example 1 were conducted except that the polymer was changed to a copolymer of poly(methylmethacrylate-methacrylic acid) (hereinafter, also referred to as P(MMA-MA), manufactured by Sigma-Aldrich Co. LLC.). The results are shown in Table 2.
  • P(MMA-MA) poly(methylmethacrylate-methacrylic acid)
  • Example 2 The same operations, measuring, and evaluation as those in Example 1 were conducted except that the polymer was changed to polymethylmethacrylate (hereinafter, also referred to as PMMA), manufactured by Sigma-Aldrich Co. LLC.). The results are shown in Table 2.
  • PMMA polymethylmethacrylate
  • Example 3 The same operations, measuring, and evaluation as those in Example 1 were conducted except that the solid content concentration of the liquid composition was changed to 58 percent by mass. The results are shown in Table 3.
  • Example 4 The same operations, measuring, and evaluation as those in Example 4 were conducted except that the dispersant for ion conductive material was changed to a basic dispersant (S13940, manufactured by Lubrizol Corporation). The results are shown in Table 3.
  • Example 4 The same operations, measuring, and evaluation as those in Example 4 were conducted except that the solvent was changed to those shown in Tables 3 to 7. The results are shown in Tables 3 to 7.
  • Example 5 The same operations, measuring, and evaluation as those in Example 5 were conducted except that a conductive assistant (acetylene black, hereinafter also referred to as AB, 1 percent by mass to the active material, manufactured by Denka Company Limited) and a basic dispersant (S13940, manufactured by Lubrizol Corporation, 20 percent by mass to the conductive assistant) as a dispersant for conductive assistant were added.
  • a conductive assistant acetylene black, hereinafter also referred to as AB, 1 percent by mass to the active material, manufactured by Denka Company Limited
  • S13940 basic dispersant manufactured by Lubrizol Corporation, 20 percent by mass to the conductive assistant
  • Example 22 The same operations, measuring, and evaluation as those in Example 22 were conducted except that the ratio of the conductive assistant to the active material was changed to 3 percent by mass and the ratio of the dispersant for conductive assistant to the active material was changed to 0.6 percent by mass. The results are shown in Table 8.
  • Example 22 The same operations, measuring, and evaluation as those in Example 22 were conducted except that the ratio of the conductive assistant to the active material was changed to 5 percent by mass and the ratio of the dispersant for conductive assistant to the active material was changed to 1.0 percent by mass. The results are shown in Table 8.
  • Example 24 The same operations, measuring, and evaluation as those in Example 24 were conducted except that the solid content concentration of the liquid composition was changed to 70 percent by mass. The results are shown in Table 9.
  • Example 25 The same operations, measuring, and evaluation as those in Example 25 were conducted except that the solvent was changed to those shown in Tables 9 to 13. The results are shown in Tables 9 to 13.
  • Example 25 The same operations, measuring, and evaluation as those in Example 25 were conducted except that a solid electrolyte was added to achieve the composition ratio shown in Table 13, the proportion of the dispersant for ion conductive material for dispersing the solid electrolyte was changed to 2.7 percent by mass, and the solvent was changed to methyl hexanoate. The results are shown in Table 13.
  • Example 43 The same operations, measuring, and evaluation as those in Example 43 were conducted except that the solvent was changed to methyl heptanoate. The results are shown in Table 13.
  • a solid electrolyte (argyrodite solid electrolyte sulfide, Li 6 PS 5 Cl(LPSC)), an acid dispersant (S13940, 5 percent by mass to the solid electrolyte, manufactured by The Lubrizol Corporation) as a dispersant for ion conductive material, and PBMA (3 percent by mass to the solid electrolyte) were mixed in a solvent (anisole) at a mass ratio to achieve a solid content concentration of 20 percent by mass based on the quantity calculated for preparation.
  • the viscosity of the liquid composition was measured according to the method described above. The evaluation results are shown in Table 14.
  • a solid electrolyte layer / positive electrode laminate for a secondary battery was manufactured in the following manner.
  • the liquid composition obtained in the manner described above was applied with an applicator to the positive electrode for secondary battery with a thickness of 100 ⁇ m (positive electrode mixture of 80 ⁇ m and aluminum foil of 20 ⁇ m) manufactured in Example 24 to achieve a solid electrolyte layer with an average film thickness of 10 ⁇ m.
  • the liquid composition on the positive electrode for secondary battery was dried in an oven at 120 degrees C to obtain a solid electrolyte layer / positive electrode laminate with a solid electrolyte layer on the positive electrode for secondary battery.
  • the film thickness's variation and the resistance to peeling of the solid electrolyte layer for a secondary battery were evaluated according to the manner described above. The evaluation results are shown in Table 14.
  • Example 45 The same operations, measuring, and evaluation as those in Example 45 were conducted except that the polymer was changed to a copolymer of poly(butylmethacrylate-methyl methacrylate) (hereinafter also referred to as P(BMA-MMA), manufactured by Sigma-Aldrich Co. LLC.) The results are shown in Table 14.
  • P(BMA-MMA) poly(butylmethacrylate-methyl methacrylate)
  • Example 45 The same operations, measuring, and evaluation as those in Example 45 were conducted except that the polymer was changed to polyethylmethacrylate (hereinafter, also referred to as PEMA), manufactured by Sigma-Aldrich Co. LLC.). The results are shown in Table 14.
  • PEMA polyethylmethacrylate
  • Example 45 The same operations, measuring, and evaluation as those in Example 45 were conducted except that the polymer was changed to a copolymer of polymethylmethacrylate-methacrylic acid) (hereinafter, also referred to as P(MMA-MA), manufactured by Sigma-Aldrich Co. LLC.). The results are shown in Table 15.
  • P(MMA-MA) polymethylmethacrylate-methacrylic acid
  • Example 45 The same operations, measuring, and evaluation as those in Example 45 were conducted except that the polymer was changed to polymethylmethacrylate (hereinafter, also referred to as PMMA), manufactured by Sigma-Aldrich Co. LLC.). The results are shown in Table 15.
  • PMMA polymethylmethacrylate
  • Example 47 The same operations, measuring, and evaluation as those in Example 47 were conducted except that the solid content concentration of the liquid composition was changed to 15 percent by mass. The results are shown in Table 16.
  • Example 47 The same operations, measuring, and evaluation as those in Example 47 were conducted except that the solid content concentration of the liquid composition was changed to 30 percent by mass. The results are shown in Table 16.
  • Example 47 The same operations, measuring, and evaluation as those in Example 47 were conducted except that the solvent was changed to xylene. The results are shown in Table 16.
  • Example 23 The same operations, measuring, and evaluation as those in Example 23 were conducted except that the polymer was changed to poly vinylidene fluoride (hereinafter, also referred to as PVdF, manufactured by Sigma-Aldrich Co. LLC.). The results are shown in Table 17.
  • PVdF poly vinylidene fluoride
  • Example 23 The same operations, measuring, and evaluation as those in Example 23 were conducted except that the polymer was changed to polyvinylidene fluoride styrene butadiene rubber (hereinafter, also referred to as SBR, manufactured by Sigma-Aldrich Co. LLC.). The results are shown in Table 17.
  • SBR polyvinylidene fluoride styrene butadiene rubber
  • Example 23 The same operations, measuring, and evaluation as those in Example 23 were conducted except that the polymer was changed to acrylonitrile butadiene rubber (hereinafter, also referred to as NBR, manufactured by Sigma-Aldrich Co. LLC.). The results are shown in Table 17.
  • NBR acrylonitrile butadiene rubber
  • a copolymer of n-butylacrylate (BA)-methyl methacrylate (MMA)-methacrylic acid(MA)-arylmethacrylate (AMA) was synthesized referring to Example 1 of WO2019/044452 .
  • the same operations, measuring, and evaluation as those in Example 7 were conducted except that the copolymer mentioned above was used and the organic solvent was changed to N-methyl-2-pyrrolidone (NMP).
  • NMP N-methyl-2-pyrrolidone
  • Each of the liquid compositions in Examples 1 to 3 contains an ion conductive material, a dispersant for ion conductive material, a polymer, which is a (meth)acrylate-based polymer with a glass transition temperature of 80 degrees C or lower, wherein the (meth)acrylate-based polymer contains a (meth)acrylic acid alkyl ester monomer, wherein the viscosity of a liquid mixture containing the polymer at 10 percent by mass and the solvent mentioned above is 50 mPa ⁇ s or less at 25 degrees C.
  • the liquid compositions have sufficiently high solid content concentration and demonstrates extremely low viscosity and can form an electrode mixture layer with high resistance to peeling.
  • Comparative Examples 1 and 2 which contain a (meth)acrylic acid alkyl ester monomer and a (meth)acrylate-based polymer with a glass transition temperature of higher than 80 degrees C, the resistance to peeling is not as good as that demonstrated in Examples 1 to 3.
  • Comparative Example 3 which contains a large amount of (meth)acrylate-based polymer with a glass transition temperature of higher than 80 degrees C, the viscosity increases, but the resistance to peeling is not good as that of Examples 1 to 3.
  • Example 4 the solid content concentration was adjusted to increase the viscosity of the liquid composition to surpass 20 mPa ⁇ s. The flow in drying the applied film was inhibited, thereby improving the variation of the film's thickness.
  • Example 5 which used a basic dispersant as a dispersant for ion conductive material, the same effect as that of Example 4 was demonstrated.
  • Example 4 The same effect as that of Example 4 was demonstrated in Examples 6 to 21 using various types of solvents.
  • thixotropy exhibits due to a solid content concentration of 60 percent by mass or greater, thereby improving the variation of film's thickness significantly.
  • Example 26 to 42 using the solvents of various types of carboxylic acid esters, the same effect as that of Example 25 was demonstrated, the viscosity further decreases, and the solid content concentration further increases.
  • the same effect as that of Example 25 was demonstrated in Examples 43 and 44 containing two or more types of ion conductive materials.
  • Example 45 to 47 using the liquid compositions prepared by using solid electrolyte sulfides as ion conductive materials, the solid content concentration of the liquid compositions sufficiently increases, the viscosity extremely decreases, and the solid electrolyte layers demonstrated high resistance to peeling as in the cases of using the liquid compositions for secondary battery in Examples 1 to 24.
  • Example 48 in which the solid content concentration was adjusted to less than 20 percent by mass, the variation in film's thickness significantly decreases in Examples 47 and 49 in which the solid content concentration was adjusted to 20 percent by mass or greater.
  • Example 50 The same effect as that of Example 47 was demonstrated in Example 50 using a xylene solvent.
  • Comparative Examples 4 and 5 which contain a (meth)acrylic acid alkyl ester monomer and a (meth)acrylate-based polymer with a glass transition temperature of higher than 80 degrees C while using solid electrolytes as the ion conductive materials, the resistance to peeling is not as good as that demonstrated in Examples 45 to 47.
  • the copolymer of n-butylacrylate (BA)-methyl methacrylate (MMA)-methacrylic acid(MA)-arylmethacrylate (AMA) disclosed in WO2019/044452 was used in Comparative Example 9.
  • the copolymer contains a polymer, which is a (meth)acrylate-based polymer with a glass transition temperature of 80 degrees C or lower.
  • the (meth)acrylate-based polymer contains a (meth)acrylic acid alkyl ester monomer.
  • the viscosity of a liquid mixture containing the polymer at 10 percent by mass and the solvent mentioned above is greater than 50 mPa ⁇ s at 25 degrees C. Its viscosity is outside the viscosity range suitable for inkjet printing.

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EP23160337.4A 2022-03-15 2023-03-07 Flüssigzusammensetzung, behälter, elektrochemisches element, verfahren und vorrichtung Pending EP4246608A1 (de)

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Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2009152180A (ja) 2007-12-18 2009-07-09 Samsung Electronics Co Ltd インクジェット印刷用電極組成物、これから得られた電極及び二次電池
WO2019044452A1 (ja) 2017-08-29 2019-03-07 日本ゼオン株式会社 非水系二次電池電極用バインダー組成物、非水系二次電池電極用スラリー組成物、非水系二次電池用電極、及び非水系二次電池
US20200199345A1 (en) * 2017-06-23 2020-06-25 Sekisui Chemical Co., Ltd. Resin composition, inorganic fine particle-dispersed slurry composition, inorganic fine particle-dispersed sheet, method for manufacturing all-solid-state battery, and method for manufacturing laminated ceramic capacitor
US20210226221A1 (en) * 2018-08-31 2021-07-22 Zeon Corporation Binder composition for all-solid-state secondary battery, slurry composition for all-solid-state secondary battery electrode mixed material layer, slurry composition for all-solid-state secondary battery solid electrolyte layer, and all-solid-state secondary battery

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2009152180A (ja) 2007-12-18 2009-07-09 Samsung Electronics Co Ltd インクジェット印刷用電極組成物、これから得られた電極及び二次電池
US20200199345A1 (en) * 2017-06-23 2020-06-25 Sekisui Chemical Co., Ltd. Resin composition, inorganic fine particle-dispersed slurry composition, inorganic fine particle-dispersed sheet, method for manufacturing all-solid-state battery, and method for manufacturing laminated ceramic capacitor
WO2019044452A1 (ja) 2017-08-29 2019-03-07 日本ゼオン株式会社 非水系二次電池電極用バインダー組成物、非水系二次電池電極用スラリー組成物、非水系二次電池用電極、及び非水系二次電池
US20210226221A1 (en) * 2018-08-31 2021-07-22 Zeon Corporation Binder composition for all-solid-state secondary battery, slurry composition for all-solid-state secondary battery electrode mixed material layer, slurry composition for all-solid-state secondary battery solid electrolyte layer, and all-solid-state secondary battery

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